APA (7th ed.) Citation

L, V. d. V., J, D. W., D, B., G, C., M, W., R, P., . . . J, B. (2022). De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia. Movement disorders : official journal of the Movement Disorder Society, 37(6), 1175. https://doi.org/10.1002/mds.28959

Chicago Style (17th ed.) Citation

L, Van de Vondel, et al. "De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia." Movement Disorders : Official Journal of the Movement Disorder Society 37, no. 6 (2022): 1175. https://doi.org/10.1002/mds.28959.

MLA (9th ed.) Citation

L, Van de Vondel, et al. "De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia." Movement Disorders : Official Journal of the Movement Disorder Society, vol. 37, no. 6, 2022, p. 1175, https://doi.org/10.1002/mds.28959.